SwePub
Sök i LIBRIS databas

  Extended search

onr:"swepub:oai:lup.lub.lu.se:25a13e2d-007b-45f2-8855-e7f98e9ea434"
 

Search: onr:"swepub:oai:lup.lub.lu.se:25a13e2d-007b-45f2-8855-e7f98e9ea434" > Two new thermostabl...

  • 1 of 1
  • Previous record
  • Next record
  •    To hitlist
  • Birgisson, HakonLund University,Lunds universitet,Bioteknik,Centrum för tillämpade biovetenskaper,Kemiska institutionen,Institutioner vid LTH,Lunds Tekniska Högskola,Biotechnology,Center for Applied Life Sciences,Department of Chemistry,Departments at LTH,Faculty of Engineering, LTH (author)

Two new thermostable alpha-L-rhamnosidases from a novel thermophilic bacterium

  • Article/chapterEnglish2004

Publisher, publication year, extent ...

  • Elsevier BV,2004

Numbers

  • LIBRIS-ID:oai:lup.lub.lu.se:25a13e2d-007b-45f2-8855-e7f98e9ea434
  • https://lup.lub.lu.se/record/140693URI
  • https://doi.org/10.1016/j.enzmictec.2003.12.012DOI

Supplementary language notes

  • Language:English
  • Summary in:English

Part of subdatabase

Classification

  • Subject category:art swepub-publicationtype
  • Subject category:ref swepub-contenttype

Notes

  • Two new thermostable alpha-L-rhamnosidases with novel substrate hydrolysis pattern were cloned and expressed from a new thermophilic bacterium. Fragments of the two alpha-L-rhamnosidase genes, rhmA and rhmB were identified in a partially sequenced genome of the bacterium. Whole genes were recovered by amplifying flanking sequences with single specific primers and nonspecific walking primers. The recovered Genes were then cloned into Escherichia coli and their enzymes produced and purified. Both enzymes were dimers and the MW of the monomers. were 104 and 107 kDa for RhmA and RhmB, respectively. Both rhamnosidases had a temperature optimum at 70degreesC. RhmA had pH optimum at 7.9 and RhmB had a broad pH optimum of 5.0 to 6.9 and RhmA had over 50% activity in the pH interval 5.0 to 8.7 and RhmB in the pH interval 4.0 to 7.9. Both enzymes had over 20% residual activity after 24-h incubation at 60degreesC. RhmA and RhmB had K values of 0.46 and 0.66 mM and V-max values of 134 and 352 U mg(-1) respectively, on p-nitrophenyl-alpha-L-rhamnopyrano side. Both rhamnosidases were active on both alpha-1,2- and alpha-1,6-linkages to beta-D-glucoside. (C) 2004 Elsevier Inc. All rights reserved.

Subject headings and genre

Added entries (persons, corporate bodies, meetings, titles ...)

  • Hreggvidsson, G O (author)
  • Fridjonsson, O H (author)
  • Mort, A (author)
  • Kristjansson, J K (author)
  • Mattiasson, BoLund University,Lunds universitet,Bioteknik,Centrum för tillämpade biovetenskaper,Kemiska institutionen,Institutioner vid LTH,Lunds Tekniska Högskola,Biotechnology,Center for Applied Life Sciences,Department of Chemistry,Departments at LTH,Faculty of Engineering, LTH(Swepub:lu)biot-bma (author)
  • BioteknikCentrum för tillämpade biovetenskaper (creator_code:org_t)

Related titles

  • In:Enzyme and Microbial Technology: Elsevier BV34:6, s. 561-5710141-0229

Internet link

Find in a library

To the university's database

  • 1 of 1
  • Previous record
  • Next record
  •    To hitlist

Find more in SwePub

By the author/editor
Birgisson, Hakon
Hreggvidsson, G ...
Fridjonsson, O H
Mort, A
Kristjansson, J ...
Mattiasson, Bo
About the subject
ENGINEERING AND TECHNOLOGY
ENGINEERING AND ...
and Industrial Biote ...
Articles in the publication
Enzyme and Micro ...
By the university
Lund University

Search outside SwePub

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Close

Copy and save the link in order to return to this view